Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 2.1 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Renal hypodysplasia/aplasia 3, OMIM:617805, Renal agenesis, MONDO:0018470 |
Component of the following Super Panels:
Signed-off version 2.1 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes CAKUT, Renal hypodysplasia/aplasia 3, 617805, inner ear malformations |